Canonical Allele Identifier: CA2195398970

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002078C= , CM000677.2:g.91002078C=	GRCh38
NC_000015.9:g.91545308C= , CM000677.1:g.91545308C=	GRCh37
NC_000015.8:g.89346312C=	NCBI36
NG_012162.1:g.25526G= , LRG_884:g.25526G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1377G= MANE Select	ENSP00000327650.4:p.Val459=
ENST00000643536.1:c.1377G=	ENSP00000494429.1:p.Val459=
ENST00000647331.1:c.1377G=	ENSP00000493953.1:p.Val459=
ENST00000333371.7:c.1377G=	ENSP00000327650.3:p.Val459=
ENST00000535906.1:c.1296G=	ENSP00000444053.1:p.Val432=
ENST00000574755.5:c.*1072G=	ENSP00000460413.1:n.*1072G=
NM_001289148.1:c.1296G=	NP_001276077.1:p.Val432=
NM_001289149.1:c.1104G=	NP_001276078.1:p.Val368=
NM_018668.4:c.1377G= , LRG_884t1:c.1377G=	NP_061138.3:p.Val459=
XM_005254884.2:c.1299G=	XP_005254941.1:p.Val433=
XM_005254887.1:c.1104G=	XP_005254944.1:p.Val368=
XM_011521448.1:c.1104G=	XP_011519750.1:p.Val368=
XM_011521449.1:c.1053G=	XP_011519751.1:p.Val351=
XM_011521449.2:c.1053G=	XP_011519751.1:p.Val351=
XM_017022075.2:c.1032G=	XP_016877564.1:p.Val344=
XM_017022076.1:c.1032G=	XP_016877565.1:p.Val344=
XR_001751213.2:n.1875G=
NM_018668.5:c.1377G= MANE Select	NP_061138.3:p.Val459=